| NDC Code | 52125-634-19 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (52125-634-19) |
|---|
| Product NDC | 52125-634 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20131031 |
|---|
| End Marketing Date | 20170810 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076194 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | LISINOPRIL; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 10; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
|---|